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Norepinephrine

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Identification
Molecular formula
C8H11NO3
CAS number
51-41-2
IUPAC name
4-[1-hydroxy-2-(isobutylamino)ethyl]benzene-1,2-diol
State
State

At room temperature, norepinephrine is typically found as a solid.

Melting point (Celsius)
217.00
Melting point (Kelvin)
490.15
Boiling point (Celsius)
342.00
Boiling point (Kelvin)
615.15
General information
Molecular weight
169.18g/mol
Molar mass
169.1770g/mol
Density
1.2980g/cm3
Appearence

The compound typically appears as colorless to white crystals or powder. It may also be observed as a pale yellow substance upon degradation or impurity. In its purest form, it is crystalline.

Comment on solubility

Solubility of 4-[1-hydroxy-2-(isobutylamino)ethyl]benzene-1,2-diol

The solubility of 4-[1-hydroxy-2-(isobutylamino)ethyl]benzene-1,2-diol is a significant aspect to consider due to its unique structural characteristics. This compound contains both hydroxyl groups and an amine, which inherently affects its interactions with solvents.

Key Factors Influencing Solubility

  • Hydrophilic Functional Groups: The presence of hydroxyl (-OH) groups typically enhances water solubility due to their ability to form hydrogen bonds with water molecules.
  • Aliphatic Chain: The isobutylamino group provides some hydrophobic characteristics, which may reduce overall solubility in polar solvents.
  • Steric Hindrance: The bulky isobutyl group may create steric hindrance, further impacting how well the molecule interacts with solvent molecules.

In conclusion, while 4-[1-hydroxy-2-(isobutylamino)ethyl]benzene-1,2-diol is expected to exhibit varying degrees of solubility based on both the hydrophilic and hydrophobic properties of its functional groups, the exact solubility in different solvents would need to be experimentally determined. Such biochemical interactions are essential to consider when formulating applications involving this compound.

Interesting facts

Interesting Facts About 4-[1-hydroxy-2-(isobutylamino)ethyl]benzene-1,2-diol

This compound, known for its complex structure, is an intriguing member of the benzene diol family. It possesses potent biological properties that pique the interest of many researchers and chemists alike. Here are some fascinating aspects of this compound:

  • Potential Medicinal Applications: This compound may play a role in drug development due to its ability to interact with various biological pathways, making it a subject of interest in the field of pharmaceuticals.
  • Structure-Activity Relationship: The presence of a hydroxyl group and an isobutylamino moiety highlights the significance of functional groups in determining the compound's reactivity and biological activity. Such variations can significantly affect the efficacy of a compound.
  • Research Significance: Studies indicate that compounds similar to this one are involved in important physiological functions, including anti-inflammatory responses and neurotransmitter modulation, which could pave the way for novel therapeutic agents.
  • Synthetic Pathways: The synthesis of this compound showcases the intricate methods used in organic chemistry, involving multiple steps that require precision and skill to yield high-purity products.

As one snippet of a larger tapestry, 4-[1-hydroxy-2-(isobutylamino)ethyl]benzene-1,2-diol exemplifies the interplay between structure, function, and potential application in various scientific arenas. With continued exploration, who knows what new discoveries await in its study?

Synonyms
WIN 5595
BRN 2728512
6924-25-0
3,4-Dihydroxy-alpha-((isobutylamino)methyl)benzyl alcohol
Protocatechuyl alcohol, alpha-(isobutylaminomethyl)-
BENZYL ALCOHOL, 3,4-DIHYDROXY-alpha-((ISOBUTYLAMINO)METHYL)-
3-13-00-02388 (Beilstein Handbook Reference)
Isopropyladrenalin
739301-51-0
SCHEMBL4847807
4-[1-Hydroxy-2-(isobutylamino)ethyl]-1,2-benzenediol
DTXSID50988960
4-{1-Hydroxy-2-[(2-methylpropyl)amino]ethyl}benzene-1,2-diolato